From natural product-inspired pyrrolidine scaffolds to the development of new human Golgi α-mannosidase II inhibitors.

about

From natural product-inspired pyrrolidine scaffolds to the development of new human Golgi α-mannosidase II inhibitors.

Item

http://www.wikidata.org/entity/Q38313410

description

2013 nî lūn-bûn

@nan

2013年の論文

@ja

2013年論文

@yue

2013年論文

@zh-hant

2013年論文

@zh-hk

2013年論文

@zh-mo

2013年論文

@zh-tw

2013年论文

@wuu

2013年论文

@zh

2013年论文

@zh-cn

name

From natural product-inspired ...... i α-mannosidase II inhibitors.

@en

type

Item

label

From natural product-inspired ...... i α-mannosidase II inhibitors.

@en

prefLabel

From natural product-inspired ...... i α-mannosidase II inhibitors.

@en

P1476

From natural product-inspired ...... i α-mannosidase II inhibitors.

@en

P2093

En-Lun Tsou

http://www.w3.org/2001/XMLSchema#string

Pei-Jung Yang

http://www.w3.org/2001/XMLSchema#string

Shang-Yu Chang

http://www.w3.org/2001/XMLSchema#string

Ting-Hao Chan

http://www.w3.org/2001/XMLSchema#string

Ting-Jen R Cheng

http://www.w3.org/2001/XMLSchema#string

Wei-Chieh Cheng

http://www.w3.org/2001/XMLSchema#string

Wen-Yi Yun

http://www.w3.org/2001/XMLSchema#string

Ying-Ta Wu

http://www.w3.org/2001/XMLSchema#string

P2860

Privileged scaffolds for library design and drug discovery

Structure of Golgi alpha-mannosidase II: a target for inhibition of growth and metastasis of cancer cells

Evaluation of docking programs for predicting binding of Golgi alpha-mannosidase II inhibitors: a comparison with crystallography

Functionalized pyrrolidine inhibitors of human type II alpha-mannosidases as anti-cancer agents: optimizing the fit to the active site

Structural analysis of Golgi alpha-mannosidase II inhibitors identified from a focused glycosidase inhibitor screen

The Molecular Basis of Inhibition of Golgi α-Mannosidase II by Mannostatin A

The evolving role of natural products in drug discovery

Combinatorial library of five-membered iminocyclitol and the inhibitory activities against glyco-enzymes.

Natural products and combinatorial chemistry: back to the future.

A quick diversity-oriented amide-forming reaction to optimize P-subsite residues of HIV protease inhibitors.

P304

2600-2604

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1002/ASIA.201300680

http://www.w3.org/2001/XMLSchema#string

P433

http://www.w3.org/2001/XMLSchema#string

P478

http://www.w3.org/2001/XMLSchema#string

P577

2013-08-13T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P698

23943613

http://www.w3.org/2001/XMLSchema#string